Method Of Treatment Or Alleviating Symptoms Of A Disorder With Cannabidiol

ABSTRACT

A method of treating or alleviating symptoms of a disorder or a condition in a subject, including identifying the disorder or the condition of a subject, the disorder or condition identified based on first measures of a bloodstream concentration of a substance or a blood stream count of cellular elements, orally administering to said subject an amount of cannabidiol over a period of time effective treat or alleviate symptoms of said disorder or said condition, altering the bloodstream concentration of said substance or said blood stream count of cellular elements, and assessing efficacy of treating or alleviating symptoms of the disorder or the condition evidenced by comparing second measures of the bloodstream concentration of the substance or the blood stream count of cellular elements after the period time to the first measures of bloodstream concentration of the substance or the blood stream count of cellular elements.

FIELD OF THE INVENTION

A method of treating or alleviating symptoms of a disorder or acondition in a subject including orally administering to the subject anamount cannabidiol effective to alter bloodstream concentration of asubstance or a blood stream count of cellular elements.

BACKGROUND OF THE INVENTION

Although there are numerous mouse and animal studies on cannabidiol(“CBD”), there are limited human studies and no credible randomizedcontrolled human studies assessing efficacy of CBD to treat or alleviatesymptoms of a disorder or a condition in a subject by orallyadministering cannabidiol in an amount effective in the subject to alterbloodstream concentration of a substance or a blood stream count ofcellular elements.

There is a long felt but unresolved need to treat or alleviate symptomsof a disorder using CBD including one or more of: a low red blood cellcount, a low eosinophil white blood cell count, a low neutrophil whiteblood cell count, a liver disorder characterized by a blood streamconcentration of alanine transaminase of 60 IU/L or higher, prediabetescharacterized by a fasting bloodstream concentration of glucose ofbetween 100 mg/dL to 125 mg/dL, and type 2 diabetes characterized by afasting bloodstream concentration of glucose of 126 mg/dL or higher.

There would be a substantial advantage in a method of treating oralleviating symptoms of a disorder or a condition by alteringbloodstream concentration of a substance or by altering a blood streamcount of cellular elements by oral administration of CBD, because CBDoffers, without a prescription, a non-toxic remedy having no known fataloverdose levels and which is virtually side effect free, outside of thetherapeutic benefit.

SUMMARY OF THE INVENTION

Accordingly, a broad object of particular embodiments of the inventioncan be to afford a method of treating or alleviating symptoms of adisorder or a condition in a subject, comprising, consisting essentiallyof, or consisting of orally administering to a subject CBD in an amounteffective in the subject to reduce bloodstream concentration of bloodglucose, blood alanine transaminase, or blood bilirubin, or combinationsthereof.

Another broad object of particular embodiments of the invention can beto afford a method of treating or alleviating symptoms of a disorder ora condition in a subject, comprising, consisting essentially of, orconsisting of orally administering to a subject CBD in an amounteffective in the subject to increase one or more of red blood cellcount, eosinophil white blood cell count and neutrophil white blood cellcount, or combinations thereof.

Another broad object of particular embodiments of the invention can beto afford a method of altering or adjusting within a normative valuerange one more of bloodstream concentration of blood glucose, bloodalanine transaminase, blood bilirubin, or one or more of red blood cellcount, eosinophil white blood cell count and neutrophil white blood cellcount.

Naturally, further objects of the invention are disclosed throughoutother areas of the specification, drawings, photographs, and claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block flow diagram of a method of treating or alleviating adisorder or condition in a subject.

DETAILED DESCRIPTION OF THE INVENTION

Generally, a method of treating or alleviating symptoms of a disorder ordisease, or of altering normative values of a condition in a subjectcomprising, consisting essentially of, or consisting of orallyadministering to a subject cannabidiol in an amount effective in thesubject to alter bloodstream concentration of a substance or a bloodstream count of cellular elements. Specifically, a method of treating oralleviating symptoms of a disorder or disease, or of altering normativevalues of a condition in a subject comprising, consisting essentiallyof, or consisting of orally administering to a subject cannabidiol in anamount effective in the subject to reduce bloodstream concentration ofone or more of: blood glucose, blood alanine transaminase, or bloodbilirubin, or effective in a subject to increase one or more of redblood cell count, eosinophil white blood cell count and neutrophil whiteblood cell count, or combinations thereof.

“A” or “an” entity means one or more of that entity; for example, “apolymer” refers to one or more polymers or at least one polymer. Assuch, the terms “a” or “an”, “one or more” and “at least one” can beused interchangeably herein. Furthermore, the language “selected fromthe group consisting of” refers to one or more of the elements in thelist that follows, including combinations of two or more of theelements.

“About” means that ranges may be expressed as from “about” oneparticular value to “about” another particular value. When such a rangeis expressed, another embodiment includes from the one particular valueto the other particular value. Similarly, when values are expressed asapproximations, by use of the antecedent “about,” it will be understoodthat the particular value forms another embodiment. In the context ofsuch a numerical value or range “about” means plus or minus 10% of thenumerical value or range recited or claimed unless otherwise specified,or the values within the range are incrementally divided into lesserpercentage between ranges or values.

“Bloodstream Concentration” for purposes of this invention means anamount of a particular substance in a specific amount of blood, andwithout sacrificing the breadth of the foregoing, can be expressed askilograms/meter3 (milligrams per deciliter (mg/dL)) or equivalentmeasure.

“Cannabidiol (CBD)” for the purposes of this invention means aphytocannabinoid having the formula C₂₁H₃₀O₂ having molar mass of314.464 g/mol and a density of 920 kg/m³ and a CAS ID 13956-29-1. CBDcan be obtained as an extract which fulfils the definition of a“botanical drug substance” provided in the Guidance for IndustryBotanical Drug Products, June 2004, US Department of Health and HumanServices, Food and Drug Administration Centre for Drug Evaluation andResearch of: “A drug substance derived from one or more plants, algae,or macroscopic fungi,”, or combinations thereof. In particularembodiments, CBD can, but need not necessarily, be extracted from abotanical biomass, such as, the stalks, stems and flowers of thecannabis sativa plant. The cannabidiol extracted from a botanicalbiomass can be a component of a full-spectrum CBD extract which includesall of the cannabinoids extracted from the botanical biomass, or can,but need not necessarily be, a CBD extract which includes only a portionof all of the cannabinoids extracted from the botanical biomass. A CBDextract of a botanical biomass can include CBD by weight occurring in arange of about 20% to about 80%. CBD can, but need not necessarily be, aCBD isolate separated from the full spectrum CBD, which CBC isolate canhave a purity in the range of up to about 99% by weight. In particularembodiments, the CBD extract or mixture of CBD extracts of a botanicalbiomass, or the CBD isolate or a mixture of CBD isolates separated froma CBD extract or mixture of extracts, or synthetic CBD, or combinationsthereof can have a weight percent occurring in the range of about 90% toabout 99%, or can be selected from the group consisting essentially ofor consisting of: about 91% to about 93%, about 92% to about 94%, about93% to about 95%, about 94% to about 96%, about 95% to about 97%, andabout 96% to about 98%. In particular embodiments the CBD extract or CBDisolate can, but need not necessarily, contain an amount oftetrahydrocannabinol (“THC”) CAS ID 1972-08-3; however, in particularembodiments the CBD extract, isolate or mixture can, but need notnecessarily, contain a weight percent THC in a range of essentially zeroto about 0.5%, and in particular embodiments, can contain a weightpercent THC of less than 0.05%. In particular embodiments, the weightpercent THC can be selected from the range of about 0.01% to about 0.1%,or a weight percent THC selected from the group consisting essentiallyof or consisting of: about 0.02% to about 0.04%, about 0.03% to about0.05%, about 0.04% to about 0.06%, about 0.05% to about 0.07%, about0.06% to about 0.08%, about 0.07% to about 0.09%. In particularembodiments, the CBD can, but need not necessarily, be chemicallysynthesized and used alone or in combination with CBD extracts or CBDisolates obtained from a botanical biomass.

“CELLg8™” is a trademark associated with a liposomal CBD productavailable from Pulpo LLC, 126 Raquette Dr. #1, Fort Collins, Colo. whichcontains CBD which may be derived from hemp in a concentration of 10mg/mL, lipids which may be derived from sunflowers, tetrahydrocannabinol<0.5%, water <1 microS/cm, and a taste mask.

“Combination or combining” for the purposes of this invention means anymethod of putting two or more materials together. Such methods include,but are not limited to, mixing, blending, commingling, concocting,dispersing, homogenizing, incorporating, intermingling, fusing, joining,shuffling, stirring, coalescing, integrating, confounding, joining,uniting, or the like.

“Complex” for the purposes of this invention means a molecular entityformed by chemical association involving two or more component molecularentities.

“Condition” for the purposes of this invention means the measurablestate of a subject whether within normative values for a particularmeasured state.

“Complete Blood Count (CBC)” for the purposes of this invention means acount of cellular elements of blood to provide measured values includingat least one of red blood cell count, eosinophil white blood cell count,or neutrophil white blood cell count.

“Comprehensive Metabolic Panel (CMP)” for the purposes of this inventionmeans chemical screen (CPT code 80053) of 16 blood tests which providesmeasured values of substances in the blood including at least one ofblood glucose, blood alanine transaminase, or blood bilirubin.

“Disorder” for the purposes of this invention means a disease or ailmentof a subject characterized by measurable values outside of the normativevalues for the subject, and without limitation to the breadth of theforegoing, includes one or more of prediabetes, diabetes, a liverdisorder characterized by high blood stream concentration of alaninetransaminase, a liver disorder characterized by high blood streamconcentration of bilirubin, low red blood cell count, low eosinophilwhite blood cell count, low neutrophil white blood cell count, orbloodstream concentration of one or more of blood glucose, blood alaninetransaminase, or blood bilirubin outside the normative values for thesubject.

“Effective” for the purposes of this invention means effecting change ina measurable value.

“Equivalent” for the purposes of this invention means a drug or chemicalcontaining similar amounts of the same ingredients as another drug orchemical or having similar chemical structures, properties or functionsto another drug or chemical.

“Hemp” for the purposes of this invention means Cannabis sativa, alsoreferred to as industrial hemp, plant of the family Cannabaceae.

“Lipid” for the purposes of this invention means a substance insolublein water and soluble in alcohol, ether, and chloroform and withoutlimitation to the breadth of the foregoing include fatty acids, neutralfats, waxes and steroids (like cortisone), compound lipids (lipidscomplexed with another type of chemical compound) including, but notnecessarily limited to, lipoproteins, glycolipids and phospholipidswhich may, but need not necessarily, be derived from botanical biomasssuch as sunflower seed, rapeseed, egg, soy, algae, or animal biomasssuch as fish, or combinations thereof.

“Liposome” for the purposes of this invention means an aggregate ofmolecules comprising at least one lipid bilayer having the nonpolarregion of the molecules of the bilayer sequestered between the polar orcharged groups of the molecules which afford an inner shell surroundingan aqueous solution core and outer shell in contact with an aqueoussolution. Hydrophilic substances dissolved in the core do not readilypass through the bilayer. Hydrophobic substances associate with thebilayer. A liposome or plurality of liposomes, whether separate or inaggregate, can be loaded with hydrophobic or hydrophilic molecules, or acombination thereof, or form a complex with hydrophobic or hydrophilicmolecules, or be combined with hydrophobic or hydrophilic molecules. Todeliver the molecules to a site of action, the lipid bilayer can fusewith other bilayers such as cell membranes, allowing delivery of theliposome contents, or complexed or combined molecules.

“Liposomal CBD” for the purposes of this invention means a liposomecontaining, complexed with or combined with an amount of CBD, andwithout sacrificing the breadth of the forgoing can be CBD contained inthe aqueous core or lipid bilayer of a liposome, CBD as a complexed witha liposome, or CBD combined with liposome even if not contained in orcomplexed with a liposome, or combinations thereof in a composition.

“Micelle” for the purposes of this invention means an aggregate ofmolecules having both polar or charged groups or molecules and nonpolarregions or molecules, where the polar or ionic groups or molecules forman outer shell in contact with a solution, and the nonpolar region ormolecules are sequestered on the interior of the shell. A micelle cancontain, be complexed with, or combined with hydrophobic or hydrophilicmolecules. To deliver the molecules to a site of action, the micelle canfuse with other bilayers such as cell membranes, allowing delivery ofthe micelle contents, or complexed or combined molecules.

“Micellular CBD” for the purposes of this invention means a micellecontaining, complexed with or combined with an amount of CBD, andwithout sacrificing the breadth of the forgoing can be CBD contained ina micelle, CBD as a complexed with a micelle, or CBD combined withliposome even if not contained in or complexed with a liposome, orcombinations thereof in a composition.

“Normative Values” for the purposes of this invention means the norm orthe standard value for a particular measured parameter and withoutlimitation to the breadth of the foregoing means a normal range ofconcentration for a particular particle or substance in the blood.

“Oral” or “Orally” for the purposes of this invention means deliveredthrough the cavity of the mouth.

“Taste Mask” for the purposes of this invention means an agent(s) usefulto mask the taste of an orally administered drug, medicament, substance,or CBD and without limitation to the foregoing, such as anethole,dihydroanethole, eugenol, wintergreen, vanillin, ethylvanillin, ethylmaltol, or the like.

“Subject” for the purposes of this invention means a human evaluated foror undergoing a method of treatment in accordance with an embodiment ofthe invention.

“Symptom” for the purposes of this invention means a physical or mentalfeature regarded as indicating a condition of a disease or a condition.

“Treating” or “Treatment” for the purposes of this invention meansmanagement and care of a subject by oral administration of CBD in anamount effective to act on or alter a disease or disorder or conditionof the subject or alleviate symptoms thereof.

Now, with primary reference to FIG. 1, the method can includeidentifying a disorder or a condition of a subject by performing firstblood tests of a subject to establish CMP or CBC baseline values (BlockM1).

The method can further include treating the disorder or condition oralleviating symptoms of the disorder or condition by orallyadministering to the subject an amount of CBD over a period of time(Block M2). In particular embodiments the amount of CBD can comprise,consist essentially of, or consist of a CBD dosage in the range of arange of 2 milligrams to about 100 milligrams. In particularembodiments, the CBD dosage can be selected from the group consistingof: about 3 milligrams to about 5 milligrams, about 4 milligrams toabout 6 milligrams, about 5 milligrams to about 7 milligrams, about 6milligrams to about 8 milligrams, about 7 milligrams to about 9milligrams, about 8 milligrams to about 10 milligrams, about 9milligrams to about 11 milligrams, about 10 milligrams to about 12milligrams, about 11 milligrams to about 13 milligrams, about 12milligrams to about 14 milligrams, about 13 milligrams to about 15milligrams, about 14 milligrams to about 16 milligrams, about 15milligrams to about 17 milligrams, about 16 milligrams to about 18milligrams, about 17 milligrams to about 19 milligrams, about 19milligrams to about 21 milligrams, about 20 milligrams to about 22milligrams, about 21 milligrams to about 23 milligrams, about 22milligrams to about 25 milligrams, about 24 milligrams to about 26milligrams, about 25 milligrams to about 27 milligrams, about 26milligrams to about 28 milligrams, about 27 milligrams to about 29milligrams, about 28 milligrams to about 30 milligrams, about 29milligrams to about 31 milligrams, about 30 milligrams to about 32milligrams, about 31 milligrams to about 33 milligrams, about 32milligrams to about 34 milligrams, about 33 milligrams to about 35milligrams, about 34 milligrams to about 36 milligrams, about 35milligrams to about 37 milligrams, about 36 milligrams to about 38milligrams, about 37 milligrams to about 39 milligrams, about 38milligrams to about 40 milligrams, about 39 milligrams to about 41milligrams, about 40 milligrams to about 42 milligrams, about 41milligrams to about 43 milligrams, about 42 milligrams to about 44milligrams, about 43 milligrams to about 45 milligrams, about 44milligrams to about 46 milligrams, about 45 milligrams to about 47milligrams, about 46 milligrams to about 48 milligrams, about 47milligrams to about 49 milligrams, about 48 milligrams to about 50milligrams, about 49 milligrams to about 51 milligrams, about 50milligrams to about 52 milligrams, about 51 milligrams to about 53milligrams, about 52 milligrams to about 54 milligrams, about 53milligrams to about 55 milligrams, about 54 milligrams to about 56milligrams, about 55 milligrams to about 57 milligrams, about 56milligrams to about 58 milligrams, about 57 milligrams to about 59milligrams, about 58 milligrams to about 60 milligrams, about 59milligrams to about 61 milligrams, about 60 milligrams to about 62milligrams, about 61 milligrams to about 63 milligrams, about 62milligrams to about 64 milligrams, about 63 milligrams to about 65milligrams, about 64 milligrams to about 66 milligrams, about 65milligrams to about 67 milligrams, about 66 milligrams to about 68milligrams, about 67 milligrams to about 69 milligrams, about 68milligrams to about 70 milligrams, about 69 milligrams to about 71milligrams, about 70 milligrams to about 72 milligrams, about 71milligrams to about 73 milligrams, about 72 milligrams to about 74milligrams, about 73 milligrams to about 75 milligrams, about 74milligrams to about 76 milligrams, about 75 milligrams to about 77milligrams, about 76 milligrams to about 78 milligrams, about 77milligrams to about 79 milligrams, about 78 milligrams to about 80milligrams, about 79 milligrams to about 81 milligrams, about 80milligrams to about 82 milligrams, about 81 milligrams to about 83milligrams, about 82 milligrams to about 84 milligrams, about 83milligrams to about 85 milligrams, about 84 milligrams to about 86milligrams, about 85 milligrams to about 87 milligrams, about 86milligrams to about 88 milligrams, about 87 milligrams to about 89milligrams, about 88 milligrams to about 90 milligrams, about 91milligrams to about 93 milligrams, about 92 milligrams to about 94milligrams, about 93 milligrams to about 95 milligrams, about 94milligrams to about 96 milligrams, about 95 milligrams to about 97milligrams, about 96 milligrams to about 98 milligrams, and about 97milligrams to about 99 milligrams.

In particular embodiments, the method can further include adjusting theCBD dosage based on the form in which the CBD is orally administeredwhether as a full spectrum CBD extract obtained from hemp, a CBDisolate, micellular CBD, liposomal CBD, CBD suspension, CBD dispersion,CELLg8™, or combinations or equivalents thereof (Block M3). As anillustrative example, oral administration of liposomal CBD or CELLg8™can provide the substantial advantage of a reduced CBD dosage. Inparticular embodiments, the CBD dosage can comprise, consist essentiallyof, or consist of liposomal CBD or CELLg8™ in the range of about 2 mg toabout 15 milligrams of CBD, and in particular embodiments the CBD dosagecan be within a range of about 8 mg to about 12 milligrams, and inparticular embodiments the CBD dosage can be about 10 mg. Thisadvantageous delivery system can be compared to full spectrum CBDextract, CBD isolate or other forms exclusive of liposomal CBD orCELLg8™ which may require substantially greater CBD dosage to afford theequivalent efficacy.

In particular embodiments, the method can further include adjusting theperiodicity of oral administration of the CBD dosage (Block M4). Theperiodicity of oral administration can vary based on the administereddosage form and CBD dosage. In particular embodiments, the periodicityof oral administration can occur within the range of three times dailyto once every seven days. In particular embodiments, the periodicity oforal administration can be selected from the group including, consistingessentially of, or consisting of: twice daily, once daily, once everytwo days, once every three days, once every four days, once every fivedays, once every six days. As one illustrative example, oraladministration of liposomal CBD or CELLg8™ containing a CBD dosage inthe range of 5 mg to 15 mg of CBD, can be orally administered once dailyto achieve efficacious results over a period of time.

In particular embodiments, the method can include adjusting a period oftime over which periodic oral administration of the CBD dosage occurs(Block M5). The period of time can be coordinated with the dosage formand CBD dosage. In particular embodiments, oral administration of a CBDdosage at a particular periodicity of administration can be maintainedindefinitely in the absence of any adverse events or side effects. Inparticular embodiments, the method can include a period of time betweenobtaining CMP or CBC baseline values and establishing one or more CMP orCBC final values after periodically orally administering a particularCBD dosage form and a particular CBD dosage for a period of time withinthe range of consecutive 15 days to 60 days. Depending on the CBD dosageform, the CBD dosage and the periodicity of oral administration, theperiod of time can be selected from the group including, consistingessentially of or consisting of: about 16 days to about 25 days, about20 days to about 30 days, about 25 days to about 35 days, about 30 daysto about 40 days, about 35 days to about 45 days, about 40 days to about50 days, about 45 days to about 55 days, and about 50 days to about 59days. As one illustrative example, in determining efficacy of once dailyoral administration of liposomal CBD or CELLg8™ at a CBD dosage of 10mg, second blood tests of the subject to establish CMP or CBC finalvalues can be performed after elapse of a period time of about 30 days.

The method can further include comparing one or more CMP or CBC finalvalues to corresponding CMP or CBC baseline values (Block M6). As oneillustrative example shown by Table 1 and by Table 2, the CMP or CBCfinal values can be compared to corresponding CMP or CBC baseline valuesrelated to the disorder or condition. In the illustrative example ofTable 1 the CMP baseline values can be compared to CMP final values andCMP normative values for each of blood glucose, blood alaninetransaminase, blood bilirubin, creatinine, or carbon dioxide, orcombinations thereof; however, this illustrative example is not intendedto preclude embodiments which include a comparison of a lesser orgreater number of CMP baseline values, CMP final values, or CMPnormative values. In the illustrative example of Table 2, the CMPbaseline values can be compared to CMP final values and CMP normativevalues for each of blood glucose, blood alanine transaminase, bloodbilirubin, creatinine, or carbon dioxide, or combinations thereof;however, this illustrative example is not intended to precludeembodiments which include a comparison of a lesser or greater number ofCMP baseline values, CMP final values, or CMP normative values.

The method can further include assessing efficacy of treating thesubject by based upon evidence of movement from CMP or CBC baselinevalues identified as the disorder or condition or symptom toward or toCMP or CBC final values within the CMP or CBC normative value or range(Block M7). With reference to Table 1, as one illustrative example, theCMP baseline value for blood glucose can be compared to CMP final valuefor blood glucose and the CMP normative range values for blood glucose.As evidenced by Table 1, in particular subjects (Participants 3, 4, 5,7, and 8), the CMP final values move closer to or within the CMPnormative range values for blood glucose evidencing efficacy of theinventive method of treatment. With reference to Table 2, as oneillustrative example, the CBC baseline value for red blood cell countcan be compared to CBC final value for red blood cell count, and the CBCnormative range values for red blood cell count. As evidenced by Table2, in particular subject (Participant 1) the CBC final value for redblood cell count moves closer to or within the CBC normative rangevalues for red blood cell count evidencing efficacy of the method oftreatment; however, this illustrative example is not intended topreclude embodiments which include a comparison of a lesser or greaternumber of CBC baseline values, CB final values, or CBC normative values.

The method can further include adjusting the amount of CBD orallyadministered to the subject over a second or more periods of time basedon assessing efficacy of prior treating the subject. Adjusting theamount of CBD can comprise one or more of changing the CBD dosage form,changing the CBD dosage, or changing the periodicity of oraladministration of the CBD dosage. As one illustrative example, the CBDdosage form and the periodicity of oral administration of the CBD dosagemay remain the same as in the prior treatment, and the CBD dosage can beincreased within the range of about 2 mg to about 100 mg.

The method can further include repeating blood tests to obtain repeatedCMP and CBC initial and final values to allow corresponding repeatedcomparison of CMP and CBC initial and final values to assess efficacy ofthe treatment of a subject using one or more embodiments of theinventive method.

EXAMPLE I.

Subjects. Subjects included ten individuals each between 25 to 70 yearsof age of generally good health and not ingesting CBD at CMP or CBCbaseline who were recruited from the general population in Colorado.Exclusion criteria for subjects included the inability to complete thetreatment protocol or the presence of a terminal illness. Subjects afterfasting for eight hours, completed a blood draw for establishing CMP anda CBC baseline values.

Disorder or Condition. The CMP and CBC baseline values evidenced thatseven out of ten of the subjects had at least one CMP or CBC baselinevalue that was above or below the normative values in the applicable CMPor CBC reference range.

Treatment. Subjects were each orally administered 10 mg of liposomal CBDonce daily for a consecutive thirty-day period without any lifestylechanges. Subjects completed a final blood draw and CMP and CBC finalvalues were compared to CMP and CBC baseline values.

Results. Of 340 blood tests that were performed on the CMP and CBCcombined, 339 remained relatively the same or improved after thirty daysof once daily oral administration of 10 mg of liposomal CBD.Additionally, seven of the ten subjects having at least one CMP or CBCbaseline value that was above or below the CMP or CBC reference rangeevidenced CMP or CBC final values that were within normative valuesafter thirty days of once daily oral administration of 10 mg ofliposomal CBD. Two subjects had a CMP or CBC final value that changedfrom normal to high at day thirty.

Table 1. Now, with reference to Table 1—CMP Measures, seven of ten ofthe CMP baseline values that were above or below the CMP normative rangenormalized after once daily oral administration of 10 mg of liposomalCBD for thirty days.

-   -   Fasting Glucose. In regard to CMP fasting glucose values, it was        observed in all five subjects that exhibited CMP baseline values        above normative glucose values (Participants 3, 4, 5, 7, and 8)        that the CMP final values evidenced a return to normative CMP        values after once daily oral administration of 10 mg of        liposomal CBD for thirty days.    -   Alanine Transaminase. In regard to CMP alanine transaminase        values, one subject (Participant 3) exhibited a CMP baseline        value for alanine transaminase outside of the CMP normative        range and that the CMP final value evidenced a return to the        normative CMP values after once daily oral administration of 10        mg of liposomal CBD for thirty days.    -   Bilirubin. In regard to CMP bilirubin values, one subject        (Participant 10) exhibited CMP baseline values for bilirubin        outside of the CMP normative value range and that the CMP final        value evidenced a return to the normative CMP value after once        daily oral administration of 10 mg of liposomal CBD for thirty        days.

Table 2. Now with reference to Table 2—CBC Measures, 5 subjects(Participants 1, 2, 4, 6 and 9) exhibited CBC baseline values outside ofCBC normative values.

Red Blood Cell Count. The CBC red blood cell count for one subject(Participant 1) exhibited CBC baseline value for red blood cell countoutside the CBC normative value and that the CBC final value evidenced areturn to the CBC normative value after once daily oral administrationof 10 mg of liposomal CBD for thirty days.

Hematocrit. The CBC hematocrit value for one subject (Participant 1)exhibited a CBC baseline value for hematocrit outside the CBC normativevalue and that the CBC final value evidenced a return to CBD normativevalues after once daily oral administration of 10 mg of liposomal CBDfor thirty days.

No Side Deleterious Side Effects. CMP and CBC values that were outsideof the normative range at CMP or CBC baseline which did not return tothe CMP or CBC normative range did not worsen. Results demonstrate thatno deleterious effects of liposomal CBD on CMP or CBC values were foundin any of the ten subjects (Participants 1-10) after once daily oraladministration of 10 mg of liposomal CBD for thirty days. Additionally,ten CMP or CBC values outside of the CMP or CBC normative range atbaseline were normalized at day thirty. This study substantiates priorreports that CBD and other cannabinoids are nontoxic and without fataloverdose levels.

In the present study, eight of ten participants maintained normalbilirubin levels; whereas one subject had their bilirubin return tonormative values over the thirty-day period. This result stands incontrast to a recent study that found hepatoxicity of CBD in a mousemodel. The present findings are also in line with other researchsuggesting that CBD may protect the liver from alcohol-induced damageand ischemia reperfusion injury.

Liposomal CBD, derived from industrial hemp, was provided as CELLg8TM.Each 1 mL contained 10 mg of CBD from full-spectrum hemp extract, lipidsderived from non-GMO sunflowers, tetrahydrocannabinol <0.05%, water <1microS/cm, with natural plant extracts used a taste mask to mask thehemp flavor.

TABLE 1 Comprehensive Metabolic Panel Measures. Change from ParticipantTest Baseline value Day 30 value Normal range baseline 2 BUN 28 mg/dL 28mg/dL 7-25 mg/dL H to H 3 Glucose 100 mg/dL 88 mg/dL 65-99 mg/dL H to N3 ALT 30 U/L 20 U/L 6-29 U/L H to N 4 Glucose 103 mg/dL 87 mg/dL 65-99mg/dL H to N 4 CO₂ 30 mmol/L 31 mmol/L 18-30 mmol/L N to H 5 Glucose 106mg/dL 94 mg/dL 65-99 mg/dL H to N 7 Glucose 109 mg/dL 91 mg/dL 65-99mg/dL H to N 8 Glucose 141 mg/dL 99 mg/dL 65-99 mg/dL H to N 10Creatinine 1.12 mg/dL 1.17 mg/dL 0.5-99 mg/dL H to H 10 Bilirubin 1.3mg/dL 1.2 mg/dL 0.5-1.2 mg/dL H to N

TABLE 2 Complete Blood Cell Count Measures Change from Participant TestBaseline value Day 30 value Normal range baseline 1 RBC count 3.95million/μL 4.28 million/μL 3.96-5.31 million/μL L to N 2 Hematocrit 39%45.6% 41.5%-53.8% L to N 2 Absolute EOC or 319 cells/μL 573 cells/μL15-500 cells/μL N to H absolute neutrophils 4 Hb 18.5 g/dL 18.4 g/dL13.7-17.7 g/dL H to H 4 MPV 13.2 f/L 13.5 f/L 7.5-12.5 f/L H to H 6 Hb11.7 g/dL 11.6 g/d 13.7-17.7 g/dL L to L 6 Hematocrit 36% 35.9%41.5%-53.8% L to L 6 MCH 26.52 pg 26.6 pg 27-33 pg L to L 6 RDW 15.6%  15.9% 11%-15% H to H 9 Absolute 617 cells/μL 536 cells/μL 850-3900cells/μL L to L lymphocytes 9 absolute EOC 9 cells/μL 8 cells/μL 15-500cells/μL L to L EOC, eosinophil count; H, high; Hb, hemoglobin; L, low;MCH, mean corpulscular hemoglobin; MPV, mean plasma volume; N, normal;RBC, red blood cell; RDW, red cell distribution width.

As can be easily understood from the foregoing, the basic concepts ofthe present invention may be embodied in a variety of ways. Theinvention involves numerous and varied embodiments of a methods fortreating a disorder or alleviating symptom of a disorder by orallyadministrating an amount of CBD over a period of time including the bestmode.

As such, the particular embodiments or elements of the inventiondisclosed by the description or shown in the figures or tablesaccompanying this application are not intended to be limiting, butrather exemplary of the numerous and varied embodiments genericallyencompassed by the invention or equivalents encompassed with respect toany particular element thereof. In addition, the specific description ofa single embodiment or element of the invention may not explicitlydescribe all embodiments or elements possible; many alternatives areimplicitly disclosed by the description and figures.

In addition, as to each term used it should be understood that unlessits utilization in this application is inconsistent with suchinterpretation, common dictionary definitions should be understood to beincluded in the description for each term as contained in the RandomHouse Webster's Unabridged Dictionary, second edition, each definitionhereby incorporated by reference.

All numeric values herein are assumed to be modified by the term“about”, whether or not explicitly indicated. For the purposes of thepresent invention, ranges may be expressed as from “about” oneparticular value to “about” another particular value. When such a rangeis expressed, another embodiment includes from the one particular valueto the other particular value. The recitation of numerical ranges byendpoints includes all the numeric values subsumed within that range. Anumerical range of one to five includes for example the numeric values1, 1.5, 2, 2.75, 3, 3.80, 4, 5, and so forth. It will be furtherunderstood that the endpoints of each of the ranges are significant bothin relation to the other endpoint, and independently of the otherendpoint. When a value is expressed as an approximation by use of theantecedent “about,” it will be understood that the particular valueforms another embodiment. The term “about” generally refers to a rangeof numeric values that one of skill in the art would consider equivalentto the recited numeric value or having the same function or result.Similarly, the antecedent “substantially” means largely, but not wholly,the same form, manner or degree and the particular element will have arange of configurations as a person of ordinary skill in the art wouldconsider as having the same function or result. When a particularelement is expressed as an approximation by use of the antecedent“substantially,” it will be understood that the particular element formsanother embodiment.

Moreover, for the purposes of the present invention, the term “a” or“an” entity refers to one or more of that entity unless otherwiselimited. As such, the terms “a” or “an”, “one or more” and “at leastone” can be used interchangeably herein.

Thus, the applicant(s) should be understood to claim at least: i)methods disclosed and described, ii) similar, equivalent, and evenimplicit variations of each of these methods, iii) those alternativeembodiments which accomplish each of the functions shown, disclosed, ordescribed, iv) those alternative designs and methods which accomplisheach of the functions shown as are implicit to accomplish that which isdisclosed and described, v) each feature, component, and step shown asseparate and independent inventions, vi) the applications enhanced bythe various systems or components disclosed, vii) the resulting productsproduced by such systems or components, viii) methods and apparatusessubstantially as described hereinbefore and with reference to any of theaccompanying examples, x) the various combinations and permutations ofeach of the previous elements disclosed.

The background section of this patent application provides a statementof the field of endeavor to which the invention pertains. This sectionmay also incorporate or contain paraphrasing of certain United Statespatents, patent applications, publications, or subject matter of theclaimed invention useful in relating information, problems, or concernsabout the state of technology to which the invention is drawn toward. Itis not intended that any United States patent, patent application,publication, statement or other information cited or incorporated hereinbe interpreted, construed or deemed to be admitted as prior art withrespect to the invention.

The claims set forth in this specification, if any, are herebyincorporated by reference as part of this description of the invention,and the applicant expressly reserves the right to use all of or aportion of such incorporated content of such claims as additionaldescription to support any of or all of the claims or any element orcomponent thereof, and the applicant further expressly reserves theright to move any portion of or all of the incorporated content of suchclaims or any element or component thereof from the description into theclaims or vice-versa as necessary to define the matter for whichprotection is sought by this application or by any subsequentapplication or continuation, division, or continuation-in-partapplication thereof, or to obtain any benefit of, reduction in feespursuant to, or to comply with the patent laws, rules, or regulations ofany country or treaty, and such content incorporated by reference shallsurvive during the entire pendency of this application including anysubsequent continuation, division, or continuation-in-part applicationthereof or any reissue or extension thereon.

Additionally, the claims set forth in this specification, if any, arefurther intended to describe the metes and bounds of a limited number ofthe preferred embodiments of the invention and are not to be construedas the broadest embodiment of the invention or a complete listing ofembodiments of the invention that may be claimed. The applicant does notwaive any right to develop further claims based upon the description setforth above as a part of any continuation, division, orcontinuation-in-part, or similar application.

What is claimed is:
 1. A method of treating or alleviating symptoms of adisorder in a subject, comprising: identifying said disorder in asubject, said disorder including a bloodstream concentration of asubstance or a blood stream count of cellular elements outside ofnormative values; orally administering to said subject an amount ofcannabidiol over a period of time effective treat or alleviate symptomsof said disorder; and altering said bloodstream concentration of saidsubstance or said blood stream count of cellular elements toward or tonormative values.
 2. The method of claim 1, wherein said disordercomprising said blood stream count of cellular elements outside ofnormative values including one or more of red blood cell count,eosinophil white blood cell count, and low neutrophil white blood cellcount.
 3. The method of claim 2, wherein said disorder comprising saidblood stream count of cellular elements outside of normative values isselected from the group consisting of: red blood cell count, eosinophilwhite blood cell count, and low neutrophil white blood cell count, orcombinations thereof.
 4. The method of claim 1, wherein said disordercomprising said bloodstream concentration of a substance outside ofnormative values including one or more of glucose, alanine transaminase,or blood bilirubin.
 5. The method of claim 1, wherein said disordercomprising said bloodstream concentration of a substance outside ofnormative values is selected from the group consisting of: glucose,alanine transaminase, or blood bilirubin, or combinations thereof. 6.The method of claim 1, wherein said disorder comprises prediabetes ordiabetes.
 7. The method of claim 6, wherein said disorder is selectedfrom the group consisting of: prediabetes characterized by a fastingbloodstream concentration of glucose of between 100mg/dL to 125 mg/dLand type 2 diabetes characterized by a fasting bloodstream concentrationof glucose of 126 mg/dL or higher.
 8. The method of claim 1, whereinsaid disorder comprises a liver disorder characterized by a blood streamconcentration outside normative range of alanine transaminase.
 9. Themethod of claim 8, wherein said disorder consisting of a liver disordercharacterized by a blood stream concentration of alanine transaminase of60 IU/L or higher.
 10. The method of claim 1, wherein said disordercomprising a liver disorder characterized by a blood streamconcentration outside normative range of bilirubin.
 11. The method ofclaim 10, wherein said disorder consisting of a liver disordercharacterized by a blood stream concentration of bilirubin of 1.2 mg/dLor higher.
 12. The method of claim 1, wherein orally administering tosaid subject an amount of cannabidiol over a period of time effectivetreat or alleviate symptoms of said disorder or said condition comprisesorally administering a dosage of cannabidiol within the range of about 2milligrams to about 100 milligrams.
 13. The method of claim 3, whereinsaid amount of cannabidiol is selected from the group consisting of:about 3 milligrams to about 5 milligrams, about 4 milligrams to about 6milligrams, about 5 milligrams to about 7 milligrams, about 6 milligramsto about 8 milligrams, about 7 milligrams to about 9 milligrams, about 8milligrams to about 10 milligrams, about 9 milligrams to about 11milligrams, about 10 milligrams to about 12 milligrams, about 11milligrams to about 13 milligrams, about 12 milligrams to about 14milligrams, about 13 milligrams to about 15 milligrams, about 14milligrams to about 16 milligrams, about 15 milligrams to about 17milligrams, about 16 milligrams to about 18 milligrams, about 17milligrams to about 19 milligrams, about 19 milligrams to about 21milligrams, about 20 milligrams to about 22 milligrams, about 21milligrams to about 23 milligrams, about 22 milligrams to about 25milligrams, about 24 milligrams to about 26 milligrams, about 25milligrams to about 27 milligrams, about 26 milligrams to about 28milligrams, about 27 milligrams to about 29 milligrams, about 28milligrams to about 30 milligrams, about 29 milligrams to about 31milligrams, about 30 milligrams to about 32 milligrams, about 31milligrams to about 33 milligrams, about 32 milligrams to about 34milligrams, about 33 milligrams to about 35 milligrams, about 34milligrams to about 36 milligrams, about 35 milligrams to about 37milligrams, about 36 milligrams to about 38 milligrams, about 37milligrams to about 39 milligrams, about 38 milligrams to about 40milligrams, about 39 milligrams to about 41 milligrams, about 40milligrams to about 42 milligrams, about 41 milligrams to about 43milligrams, about 42 milligrams to about 44 milligrams, about 43milligrams to about 45 milligrams, about 44 milligrams to about 46milligrams, about 45 milligrams to about 47 milligrams, about 46milligrams to about 48 milligrams, about 47 milligrams to about 49milligrams, about 48 milligrams to about 50 milligrams, about 49milligrams to about 51 milligrams, about 50 milligrams to about 52milligrams, about 51 milligrams to about 53 milligrams, about 52milligrams to about 54 milligrams, about 53 milligrams to about 55milligrams, about 54 milligrams to about 56 milligrams, about 55milligrams to about 57 milligrams, about 56 milligrams to about 58milligrams, about 57 milligrams to about 59 milligrams, about 58milligrams to about 60 milligrams, about 59 milligrams to about 61milligrams, about 60 milligrams to about 62 milligrams, about 61milligrams to about 63 milligrams, about 62 milligrams to about 64milligrams, about 63 milligrams to about 65 milligrams, about 64milligrams to about 66 milligrams, about 65 milligrams to about 67milligrams, about 66 milligrams to about 68 milligrams, about 67milligrams to about 69 milligrams, about 68 milligrams to about 70milligrams, about 69 milligrams to about 71 milligrams, about 70milligrams to about 72 milligrams, about 71 milligrams to about 73milligrams, about 72 milligrams to about 74 milligrams, about 73milligrams to about 75 milligrams, about 74 milligrams to about 76milligrams, about 75 milligrams to about 77 milligrams, about 76milligrams to about 78 milligrams, about 77 milligrams to about 79milligrams, about 78 milligrams to about 80 milligrams, about 79milligrams to about 81 milligrams, about 80 milligrams to about 82milligrams, about 81 milligrams to about 83 milligrams, about 82milligrams to about 84 milligrams, about 83 milligrams to about 85milligrams, about 84 milligrams to about 86 milligrams, about 85milligrams to about 87 milligrams, about 86 milligrams to about 88milligrams, about 87 milligrams to about 89 milligrams, about 88milligrams to about 90 milligrams, about 91 milligrams to about 93milligrams, about 92 milligrams to about 94 milligrams, about 93milligrams to about 95 milligrams, about 94 milligrams to about 96milligrams, about 95 milligrams to about 97 milligrams, about 96milligrams to about 98 milligrams, and about 97 milligrams to about 99milligrams.
 14. The method of claim 12, wherein said amount ofcannabidiol contained in a plant biomass extract.
 15. The method ofclaim 11, wherein said amount of cannabidiol contained in a hempextract.
 16. The method of claim 14, wherein said hemp extract containssaid cannabidiol in a concentration of about 5 mg/mL to about 15 mg/mL.17. The method of claim 15, wherein said hemp extract contains saidcannabidiol in a concentration selected from the group consisting of:about 6 mg/mL to about 8 mg/mL, about 7 mg/mL to about 9 mg/mL, about 8mg/mL to about 10 mg/mL, about 9 mg/mL to about 11 mg/mL, about 10 mg/mLto about 12 mg/mL, about 11 mg/mL to about 13 mg/mL, and about 12 mg/mLto about 14 mg/mL.
 18. The method of claim 12, further comprising lipidsadmixed with said amount of cannabidiol.
 19. The method of claim 15,wherein said lipids are obtained from the group consisting of: plantbiomass or animal biomass.
 20. The method of claim 15, wherein saidlipids admixed with said amount of cannabidiol forms CBD liposomes orCBD micelles.
 21. The method of claim 12, wherein said cannabidiolcomprises a composition, including: a hemp extract containing saidcannabidiol in a range of about 5 mg/mL to about 15 mg/mL; lipids;tetrahydrocannabinol <0.05% by weight; and water <1 μS/cm.
 22. Themethod of claim 21, further comprising a taste mask.
 23. The method ofclaim 22, wherein said composition including said cannabidiol comprisesLiposomal CELLg8 CBD.
 24. The method of claim 23, wherein said mixtureincluding said cannabidiol consists of Liposomal CELLg8 CBD.
 25. Amethod of treating or alleviating symptoms of a condition in a subject,the method comprising: identifying said condition in a subject, saidcondition including a bloodstream concentration of a substance or ablood stream count of cellular elements within a range of normativevalues; orally administering to said subject an amount of cannabidiolover a period of time effective treat or alleviate symptoms of saidcondition; and altering said bloodstream concentration of said substanceor said blood stream count of cellular elements to within said range ofnormative values.